HGVS | Genome Assembly |
---|---|
NC_000008.11:g.98158185C>T , CM000670.2:g.98158185C>T | GRCh38 |
NC_000008.10:g.99170413C>T , CM000670.1:g.99170413C>T | GRCh37 |
NC_000008.9:g.99239589C>T | NCBI36 |
NG_052869.1:g.45893C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401707.7:c.2989C>T MANE Select | ENSP00000385787.2:p.Gln997Ter | |
ENST00000349693.3:c.2989C>T | ENSP00000339529.3:p.Gln997Ter | |
ENST00000401707.6:c.2989C>T | ENSP00000385787.2:p.Gln997Ter | |
NM_001145860.1:c.2989C>T | NP_001139332.1:p.Gln997Ter | |
NM_001145861.1:c.2989C>T | NP_001139333.1:p.Gln997Ter | |
NM_015029.2:c.2989C>T | NP_055844.2:p.Gln997Ter | |
NM_001145860.2:c.2989C>T MANE Select | NP_001139332.1:p.Gln997Ter | |
NM_001145861.2:c.2989C>T | NP_001139333.1:p.Gln997Ter | |
NM_015029.3:c.2989C>T | NP_055844.2:p.Gln997Ter |